Xie WJ - Search Results

1

Synthesis and β-adrenergic blocking activity of oxime ether hybrids derived from a natural isochroman-4-one.

Bai RR, Xu ST, Liu J, Hong W, Tang YQ, Wu XM, Xie WJ, Yao HQ, Xu JY. Bai RR, et al. Among authors: xie wj. Chin J Nat Med. 2013 Sep;11(5):538-45. doi: 10.1016/S1875-5364(13)60098-9. Chin J Nat Med. 2013. PMID: 24359781

2

Synthesis and biological evaluation of 4'-[(benzimidazole-1-yl)methyl]biphenyl-2-sulfonamide derivatives as dual angiotensin II/endothelin A receptor antagonists.

Bai R, Wei Z, Liu J, Xie W, Yao H, Wu X, Jiang J, Wang Q, Xu J. Bai R, et al. Bioorg Med Chem. 2012 Aug 1;20(15):4661-7. doi: 10.1016/j.bmc.2012.06.011. Epub 2012 Jun 15. Bioorg Med Chem. 2012. PMID: 22750010

3

Novel nitric oxide-releasing isochroman-4-one derivatives: Synthesis and evaluation of antihypertensive activity.

Bai R, Yang X, Zhu Y, Zhou Z, Xie W, Yao H, Jiang J, Liu J, Shen M, Wu X, Xu J. Bai R, et al. Bioorg Med Chem. 2012 Dec 1;20(23):6848-55. doi: 10.1016/j.bmc.2012.09.043. Epub 2012 Sep 28. Bioorg Med Chem. 2012. PMID: 23084434

4

Total synthesis of neokotalanol, a potent α-glucosidase inhibitor isolated from Salacia reticulata.

Xie WJ, Tanabe G, Tsutsui N, Wu XM, Muraoka O. Xie WJ, et al. Chin J Nat Med. 2013 Nov;11(6):676-83. doi: 10.1016/S1875-5364(13)60079-5. Chin J Nat Med. 2013. PMID: 24345510

5

Construction of 3,6-anhydrohexosides via intramolecular cyclization of triflates and its application to the synthesis of natural product isolated from leaves of Sauropus rostratus.

Liu L, Wang CQ, Liu D, He WG, Xu JY, Lin AJ, Yao HQ, Tanabe G, Muraoka O, Xie WJ, Wu XM. Liu L, et al. Among authors: xie wj. Org Lett. 2014 Oct 3;16(19):5004-7. doi: 10.1021/ol5022838. Epub 2014 Sep 15. Org Lett. 2014. PMID: 25221862

6

Design, synthesis and biological evaluation of 3'-benzylated analogs of 3'-epi-neoponkoranol as potent α-glucosidase inhibitors.

Liu D, He W, Wang Z, Liu L, Wang C, Zhang C, Wang C, Wang Y, Tanabe G, Muraoka O, Wu X, Wu L, Xie W. Liu D, et al. Eur J Med Chem. 2016 Mar 3;110:224-36. doi: 10.1016/j.ejmech.2016.01.029. Epub 2016 Jan 22. Eur J Med Chem. 2016. PMID: 26840363

7

Probing the Anticancer Action of Oridonin with Fluorescent Analogues: Visualizing Subcellular Localization to Mitochondria.

Xu S, Luo S, Yao H, Cai H, Miao X, Wu F, Yang DH, Wu X, Xie W, Yao H, Chen ZS, Xu J. Xu S, et al. J Med Chem. 2016 May 26;59(10):5022-34. doi: 10.1021/acs.jmedchem.6b00408. Epub 2016 Apr 27. J Med Chem. 2016. PMID: 27089099

8

Total synthesis, structural elucidation and anti-inflammatory activity evaluation of 2-deoxy-3,6-anhydro hexofuranoside derivatives isolated from Sauropus rostratus.

Zhang C, Wang C, Wang Z, Tanabe G, Muraoka O, Lin A, Xu J, Wu X, Wu L, Xie W. Zhang C, et al. Org Biomol Chem. 2016 Nov 22;14(46):10906-10913. doi: 10.1039/c6ob02207c. Org Biomol Chem. 2016. PMID: 27814424

9

A Novel Potent Anticancer Compound Optimized from a Natural Oridonin Scaffold Induces Apoptosis and Cell Cycle Arrest through the Mitochondrial Pathway.

Xu S, Yao H, Luo S, Zhang YK, Yang DH, Li D, Wang G, Hu M, Qiu Y, Wu X, Yao H, Xie W, Chen ZS, Xu J. Xu S, et al. J Med Chem. 2017 Feb 23;60(4):1449-1468. doi: 10.1021/acs.jmedchem.6b01652. Epub 2017 Feb 13. J Med Chem. 2017. PMID: 28165738

10

Design, synthesis and biological evaluation of novel nitric oxide-donating protoberberine derivatives as antitumor agents.

Chen J, Wang T, Xu S, Lin A, Yao H, Xie W, Zhu Z, Xu J. Chen J, et al. Eur J Med Chem. 2017 May 26;132:173-183. doi: 10.1016/j.ejmech.2017.03.027. Epub 2017 Mar 18. Eur J Med Chem. 2017. PMID: 28359045

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